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1,1-dimethoxy-N-methyl-propan-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65765-12-0 Structure
  • Basic information

    1. Product Name: 1,1-dimethoxy-N-methyl-propan-2-amine
    2. Synonyms:
    3. CAS NO:65765-12-0
    4. Molecular Formula:
    5. Molecular Weight: 133.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65765-12-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,1-dimethoxy-N-methyl-propan-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-dimethoxy-N-methyl-propan-2-amine(65765-12-0)
    11. EPA Substance Registry System: 1,1-dimethoxy-N-methyl-propan-2-amine(65765-12-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 65765-12-0(Hazardous Substances Data)

65765-12-0 Usage

Class

Substituted amphetamines

Psychoactive substance

Yes

Central nervous system stimulant

Yes

Effects

Increased energy, alertness, and euphoria

Structural relation

Related to methamphetamine

Potency

Less potent than methamphetamine

Duration of action

Shorter than methamphetamine

Medical use

Not approved

Recreational use

Yes, often in designer drugs or as a research chemical

Effects and safety profile

Not well-studied

Health risks

Potential risks associated with use

Legal issues

Use may be associated with legal issues

Availability

Not for medical use, primarily for recreational or research purposes

Check Digit Verification of cas no

The CAS Registry Mumber 65765-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,6 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65765-12:
(7*6)+(6*5)+(5*7)+(4*6)+(3*5)+(2*1)+(1*2)=150
150 % 10 = 0
So 65765-12-0 is a valid CAS Registry Number.

65765-12-0Downstream Products

65765-12-0Relevant articles and documents

Herbicidal Compounds

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Paragraph 0215; 0216; 0217, (2017/11/30)

The invention relates to substituted pyrrolone derivatives of the formula (I) wherein X, A, R1, R2 and R3 are as defined in the specification. Furthermore, the present invention relates to processes and intermediates for making compounds of formula (I), to herbicidal compositions comprising these compounds and to methods of using these compounds to control or inhibit plant growth.

HERBICIDAL MIXTURES

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Page/Page column 40; 45, (2016/10/31)

The present invention provides a composition comprising (A) a compound of formula (I): wherein R1 is methyl or methoxy, R2 is hydrogen, methyl or ethoxy and A is a substituted heteroaryl group, or an N-oxide or salt form thereof, and

HERBICIDAL COMPOUNDS

-

Page/Page column 49, (2015/04/28)

The invention relates to pyrrolone compounds of the formula (I), wherein X, R1, R2, R3, Ra, Rb, Rc and Rd are as defined in the specification. Furthermore, the present invention

1 -(PYRIDAZIN-3-YL)-IMIDAZOLIDIN-2-ONE DERIVATIVES AS HERBICIDES

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Page/Page column 34, (2015/05/26)

The invention relates to pyrrolone compounds of the formula (I) wherein R1, R2, R3, Rb, Rc and Rd are as defined in the specification. Furthermore, the present invention relates to processe

DIHYDRO-HYDANTOIN DERIVATIVES WITH HERBICIDAL ACTIVITY

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Page/Page column 37; 38, (2015/07/15)

The invention relates to substituted dihydro-hydantoin derivatives of the formula (I) wherein X, Ra, Rb, Rc, R1, R2 and R3 are as defined in the specification. Furthermore, the present invention relates to processes and intermediates for making compounds of formula (I), to herbicidal compositions comprising these compounds and to methods of using these compounds 10 to control or inhibit plant growth.

Synthesis of N-methyl secondary amines

Kumpaty, Hephzibah J.,Williamson, John S.,Bhattacharyya, Sukanta

, p. 1411 - 1416 (2007/10/03)

A diverse set of N-methyl secondary amines are obtained in high yields by an expedient reductive alkylation of commercially available methanolic methylamine.

Facile preparation of N-methyl secondary amines by titanium(IV) isopropoxide-mediated reductive animation of carbonyl compounds

Neidigh, Kurt A.,Avery, Mitchell A.,Williamson, John S.,Bhattacharyya, Sukanta

, p. 2527 - 2531 (2007/10/03)

A simple, mild and efficient procedure for obtaining N-methyl secondary amines from aldehydes and ketones is reported. Treatment of carbonyl compounds with methylamine hydrochloride, triethylamine and titanium(IV) isopropoxide, followed by in situ sodium borohydride reduction and straightforward aqueous work-up, affords clean products in good to excellent yields.

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